| Chemical Name: | 2-methoxy-5-(3-oxo-1H-isoindol-2-yl)benzenesulfonyl chloride |
| CAS Number: | 126565-42-2 |
| Product Number: | AG000SYA(AGN-PC-0LDZV2) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C15H12ClNO4S |
| Molecular Weight: | 337.7781 |
2-Methoxy-5-(1-oxoisoindolin-2-yl)benzene-1-sulfonyl chloride, also known as $name$, serves as a versatile reagent in chemical synthesis due to its unique structure and reactivity. This compound is commonly employed in the preparation of various organic molecules through the introduction of functional groups and modifications.One of the key applications of $name$ in chemical synthesis is as a sulfonylating agent. By utilizing the sulfonyl chloride group, chemists can introduce the sulfonyl functionality into organic molecules, which can serve as a useful handle for further derivatization. This allows for the selective and efficient modification of complex molecules, enabling the synthesis of diverse chemical structures.Additionally, $name$ can be utilized in the synthesis of biologically active compounds and pharmaceuticals. The sulfonyl chloride moiety in $name$ can participate in a range of reactions, including nucleophilic substitutions, facilitating the construction of complex molecular scaffolds present in many pharmaceutical agents.Overall, the application of 2-Methoxy-5-(1-oxoisoindolin-2-yl)benzene-1-sulfonyl chloride in chemical synthesis enables chemists to access new chemical entities with tailored properties and functionalities, making it a valuable tool in organic chemistry research and drug discovery efforts.
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